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FDA Grants Toripalimab Fast Track Designation for Mucosal Melanoma
FDA Grants Toripalimab Fast Track Designation for Mucosal Melanoma
SHANGHAI, China, Jan.
FDA Approves Aurinia Pharmaceuticals’ LUPKYNIS™ (voclosporin) for Adult Patients with Active Lupus Nephritis
FDA Approves Aurinia Pharmaceuticals’ LUPKYNIS™ (voclosporin) for Adult Patients with Active Lupus Nephritis
VICTORIA, British Columbia & ROCKVILLE, Md.
CDC study says Abbott's rapid COVID-19 antigen test may miss two-thirds of asymptomatic cases
CDC study says Abbott's rapid COVID-19 antigen test may miss two-thirds of asymptomatic cases
Shortly after Abbott completed its delivery of 150 million rapid antigen tests to the federal government for widespread distribution against the COVID-19 pandemic, researchers at the Centers for Disea...
Eli Lilly’s Loxo Oncology Enters into $1.6 Billion Research and Collaboration Agreement with Merus N.V.
Eli Lilly’s Loxo Oncology Enters into $1.6 Billion Research and Collaboration Agreement with Merus N.V.
Loxo Oncology at Lilly, a research and development group of Eli Lilly and Company and Merus N.
Janssen Announces U.S. FDA Approval of CABENUVA (rilpivirine and cabotegravir), the First Long-Acting Regimen for the Treatment of HIV
Janssen Announces U.S. FDA Approval of CABENUVA (rilpivirine and cabotegravir), the First Long-Acting Regimen for the Treatment of HIV
TITUSVILLE, N.
Servier and MiNA Partner to Create Entirely New Class of Drugs
Servier and MiNA Partner to Create Entirely New Class of Drugs
France-based Servier and U.
Boston Scientific Announces Agreement To Acquire Preventice Solutions, Inc.
Boston Scientific Announces Agreement To Acquire Preventice Solutions, Inc.
MARLBOROUGH, Mass.
Merck Announces U.S. FDA Approval of VERQUVO® (vericiguat)
Merck Announces U.S. FDA Approval of VERQUVO® (vericiguat)
KENILWORTH, NJ, USA I January 20, 2021 I Merck (NYSE.
FDA Grants Priority Review to Genentech’s Esbriet (pirfenidone) for Unclassifiable Interstitial Lung Disease
FDA Grants Priority Review to Genentech’s Esbriet (pirfenidone) for Unclassifiable Interstitial Lung Disease
SOUTH SAN FRANCISCO, CA, USA, January 21, 2021.
Monoclonal antibody treatment by Eli Lilly found to cut risk of serious COVID-19, drugmaker reports
Monoclonal antibody treatment by Eli Lilly found to cut risk of serious COVID-19, drugmaker reports
A drug developed by Eli Lilly and Company dramatically reduced the risk of developing symptomatic COVID-19 among nursing home residents, the company found.
Mark Cuban launches low-cost generic drug company
Mark Cuban launches low-cost generic drug company
Billionaire Mark Cuban launched a drug company this week that is “dedicated to producing low-cost versions of high-cost generic drugs” and pledges “radical transparency” in pricing.
Doptelet® (avatrombopag) approved in the EU for treatment of ITP
Doptelet® (avatrombopag) approved in the EU for treatment of ITP
STOCKHOLM, Sweden I January 20, 2021 ISwedish Orphan Biovitrum AB (publ) (Sobi™) (STO.
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